rs1800206, PPARA

N. diseases: 35
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
HYPERAPOBETALIPOPROTEINEMIA, SUSCEPTIBILITY TO
1 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.700 0
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2016 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2017 2017
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2008 2008
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2011 2011
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2016 2016
Dystrophia myotonica 2
CUI: C2931689
Disease: Dystrophia myotonica 2
21 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2004 2004
Fatty Liver
CUI: C0015695
Disease: Fatty Liver
35 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2005 2005
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
81 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2005 2005
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2011 2011
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2005 2005
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
28 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2002 2002
Lipid Metabolism Disorders
CUI: C0154251
Disease: Lipid Metabolism Disorders
10 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2002 2002
Lipodystrophy
CUI: C0023787
Disease: Lipodystrophy
28 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1 2012 2012
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1 2008 2008
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2017 2017
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2009 2009
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2002 2002
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2013 2013
Nonalcoholic Steatohepatitis
CUI: C3241937
Disease: Nonalcoholic Steatohepatitis
17 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2005 2005
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
75 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2005 2005
Tumor Progression
CUI: C0178874
Disease: Tumor Progression
72 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2008 2008
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.020 1.000 2 2003 2009
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.020 1.000 2 2002 2004
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.020 1.000 2 2002 2004